Canonical Allele Identifier: CA414858692

Gene: RPS4Y2

Linked Data

• MyVariant Identifiers: chrY:g.22921888T>G (hg19) ; chrY:g.20760002T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.20760002T>G , CM000686.2:g.20760002T>G	GRCh38
NC_000024.9:g.22921888T>G , CM000686.1:g.22921888T>G	GRCh37
NC_000024.8:g.21331276T>G	NCBI36
NG_032924.1:g.8935T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000629237.2:c.216T>G MANE Select	ENSP00000486252.1:p.Ile72Met
ENST00000629237.1:c.216T>G	ENSP00000486252.1:p.Ile72Met
NM_001039567.2:c.216T>G	NP_001034656.1:p.Ile72Met
XM_011531423.1:c.165T>G	XP_011529725.1:p.Ile55Met
NM_001039567.3:c.216T>G MANE Select	NP_001034656.1:p.Ile72Met